MA31296B1 - Derives d'imidazolidine carboxamide en tant qu'inhibiteurs de lipase et de phospholipase - Google Patents
Derives d'imidazolidine carboxamide en tant qu'inhibiteurs de lipase et de phospholipaseInfo
- Publication number
- MA31296B1 MA31296B1 MA32251A MA32251A MA31296B1 MA 31296 B1 MA31296 B1 MA 31296B1 MA 32251 A MA32251 A MA 32251A MA 32251 A MA32251 A MA 32251A MA 31296 B1 MA31296 B1 MA 31296B1
- Authority
- MA
- Morocco
- Prior art keywords
- imidazolidin
- lipase
- carboxamide derivatives
- phospholipase inhibitors
- phospholipase
- Prior art date
Links
- NTFOMPCTOJCWEK-UHFFFAOYSA-N imidazolidine-1-carboxamide Chemical class NC(=O)N1CCNC1 NTFOMPCTOJCWEK-UHFFFAOYSA-N 0.000 title abstract 2
- 102000004882 Lipase Human genes 0.000 title 1
- 108090001060 Lipase Proteins 0.000 title 1
- 239000004367 Lipase Substances 0.000 title 1
- 235000019421 lipase Nutrition 0.000 title 1
- 239000003428 phospholipase inhibitor Substances 0.000 title 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61P17/04—Antipruritics
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P35/00—Antineoplastic agents
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Vascular Medicine (AREA)
- Psychology (AREA)
- Reproductive Health (AREA)
- Ophthalmology & Optometry (AREA)
Abstract
La présente invention concerne des dérivés d'amide d'acide imidazolidine-carboxylique de formule générale (i), dans laquelle les substituants ont les significations indiquées dans la description, ainsi que leurs sels pharmaceutiquement acceptables et leur utilisation comme substances pharmaceutiques.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07007161 | 2007-04-05 | ||
| PCT/EP2008/002231 WO2008122352A1 (fr) | 2007-04-05 | 2008-03-20 | Dérivés d'amide d'acide imidazolidine-carboxylique utilisés comme inhibiteurs de lipases et de phospholipases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31296B1 true MA31296B1 (fr) | 2010-04-01 |
Family
ID=38169713
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32251A MA31296B1 (fr) | 2007-04-05 | 2009-10-02 | Derives d'imidazolidine carboxamide en tant qu'inhibiteurs de lipase et de phospholipase |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8735437B2 (fr) |
| EP (1) | EP2144885B1 (fr) |
| JP (1) | JP2010523503A (fr) |
| KR (1) | KR20090126293A (fr) |
| CN (1) | CN101646655A (fr) |
| AR (1) | AR065932A1 (fr) |
| AU (1) | AU2008235066A1 (fr) |
| BR (1) | BRPI0809693A2 (fr) |
| CA (1) | CA2682875A1 (fr) |
| CL (1) | CL2008000981A1 (fr) |
| CO (1) | CO6220934A2 (fr) |
| IL (1) | IL201255A0 (fr) |
| MA (1) | MA31296B1 (fr) |
| MX (1) | MX2009010485A (fr) |
| NZ (1) | NZ580127A (fr) |
| RU (1) | RU2009140761A (fr) |
| TW (1) | TW200904804A (fr) |
| UY (1) | UY31001A1 (fr) |
| WO (1) | WO2008122352A1 (fr) |
| ZA (1) | ZA200906211B (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011107494A1 (fr) | 2010-03-03 | 2011-09-09 | Sanofi | Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation |
| WO2011157827A1 (fr) | 2010-06-18 | 2011-12-22 | Sanofi | Dérivés d'azolopyridin-3-one en tant qu'inhibiteurs de lipases et de phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| WO2013037390A1 (fr) | 2011-09-12 | 2013-03-21 | Sanofi | Dérivés amides d'acide 6-(4-hydroxyphényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase |
| EP2760862B1 (fr) | 2011-09-27 | 2015-10-21 | Sanofi | Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique utilisés comme inhibiteurs de kinase |
| EP2760830B1 (fr) * | 2011-09-27 | 2016-08-03 | Bristol-Myers Squibb Company | Dérivés de pyrrolinone-carboxamide utiles comme inhibiteurs de lipase endothéliale |
| US8952180B2 (en) | 2011-09-27 | 2015-02-10 | Bristol-Myers Squibb Company | Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors |
| EP2760828B1 (fr) | 2011-09-27 | 2015-10-21 | Bristol-Myers Squibb Company | Composés de pyrrolinone-carboxamide utiles en tant qu'inhibiteurs de lipase endothéliale |
| US8933235B2 (en) | 2011-09-30 | 2015-01-13 | Bristol-Myers Squibb Company | Pyridinedione carboxamide inhibitors of endothelial lipase |
| US9199946B2 (en) | 2012-04-03 | 2015-12-01 | Bristol-Myers Squibb Company | Pyrimidinone carboxamide inhibitors of endothelial lipase |
| WO2013151923A1 (fr) * | 2012-04-03 | 2013-10-10 | Bristol-Myers Squibb Company | Pyrimidinone carboxamides en tant qu'inhibiteurs d'une lipase endothéliale |
| AR102942A1 (es) | 2014-12-11 | 2017-04-05 | Bayer Cropscience Ag | Derivados de arilsulfuro y arilsulfóxido de cinco miembros c-n-conectados, como plaguicidas |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03227976A (ja) * | 1990-02-01 | 1991-10-08 | Otsuka Chem Co Ltd | イミダゾリジン―2―オン誘導体 |
| JP3227976B2 (ja) | 1993-02-26 | 2001-11-12 | 松下電器産業株式会社 | 光学的情報記録部材、記録再生方法、及び記録再生装置 |
| JP3947283B2 (ja) | 1997-11-19 | 2007-07-18 | 株式会社堀場製作所 | イプロジオン及びその代謝物のハプテン化合物、抗体及び測定方法 |
| US6500839B2 (en) * | 2000-05-18 | 2002-12-31 | Neurocrine Biosciences, Inc. | CRF receptor antagonists and methods relating thereto |
| EP1610779B1 (fr) | 2003-03-31 | 2009-09-09 | Eli Lilly And Company | Utilisation de derives amides d'acide 3-oxo-1,3-dihydro-indazole-2-carboxylique comme inhibiteurs de la phospholipase |
| US7217727B2 (en) | 2003-04-01 | 2007-05-15 | Eli Lilly And Company | Phospholipase inhibitors |
| US7595403B2 (en) | 2003-04-01 | 2009-09-29 | Eli Lilly And Company | Benzisothiazol-3-one-carboxylic acid amides as phospholipase inhibitors |
| US20090253908A1 (en) * | 2004-03-11 | 2009-10-08 | Glaxo Group Limited | Novel m3 muscarinic acetylchoine receptor antagonists |
| DE102005018389A1 (de) | 2005-04-20 | 2006-10-26 | Sanofi-Aventis Deutschland Gmbh | Azolderivate als Inhibitoren von Lipasen und Phospholipasen |
-
2008
- 2008-03-20 KR KR1020097020794A patent/KR20090126293A/ko not_active Withdrawn
- 2008-03-20 EP EP08734683.9A patent/EP2144885B1/fr active Active
- 2008-03-20 JP JP2010501401A patent/JP2010523503A/ja not_active Withdrawn
- 2008-03-20 CN CN200880009966A patent/CN101646655A/zh active Pending
- 2008-03-20 CA CA002682875A patent/CA2682875A1/fr not_active Abandoned
- 2008-03-20 NZ NZ580127A patent/NZ580127A/en unknown
- 2008-03-20 AU AU2008235066A patent/AU2008235066A1/en not_active Abandoned
- 2008-03-20 MX MX2009010485A patent/MX2009010485A/es unknown
- 2008-03-20 RU RU2009140761/04A patent/RU2009140761A/ru not_active Application Discontinuation
- 2008-03-20 WO PCT/EP2008/002231 patent/WO2008122352A1/fr not_active Ceased
- 2008-03-20 BR BRPI0809693-7A2A patent/BRPI0809693A2/pt not_active Application Discontinuation
- 2008-04-02 TW TW097111925A patent/TW200904804A/zh unknown
- 2008-04-03 AR ARP080101389A patent/AR065932A1/es unknown
- 2008-04-03 UY UY31001A patent/UY31001A1/es not_active Application Discontinuation
- 2008-04-04 CL CL200800981A patent/CL2008000981A1/es unknown
-
2009
- 2009-09-08 ZA ZA200906211A patent/ZA200906211B/xx unknown
- 2009-09-30 IL IL201255A patent/IL201255A0/en unknown
- 2009-09-30 CO CO09107074A patent/CO6220934A2/es not_active Application Discontinuation
- 2009-10-02 MA MA32251A patent/MA31296B1/fr unknown
- 2009-10-02 US US12/572,462 patent/US8735437B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008235066A1 (en) | 2008-10-16 |
| WO2008122352A1 (fr) | 2008-10-16 |
| CL2008000981A1 (es) | 2008-10-10 |
| NZ580127A (en) | 2011-03-31 |
| RU2009140761A (ru) | 2011-05-10 |
| ZA200906211B (en) | 2010-05-26 |
| US8735437B2 (en) | 2014-05-27 |
| KR20090126293A (ko) | 2009-12-08 |
| AR065932A1 (es) | 2009-07-08 |
| MX2009010485A (es) | 2009-10-19 |
| TW200904804A (en) | 2009-02-01 |
| EP2144885A1 (fr) | 2010-01-20 |
| US20100105719A1 (en) | 2010-04-29 |
| EP2144885B1 (fr) | 2016-06-29 |
| CO6220934A2 (es) | 2010-11-19 |
| CN101646655A (zh) | 2010-02-10 |
| CA2682875A1 (fr) | 2008-10-16 |
| IL201255A0 (en) | 2010-05-31 |
| JP2010523503A (ja) | 2010-07-15 |
| BRPI0809693A2 (pt) | 2014-10-07 |
| UY31001A1 (es) | 2008-11-28 |
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| MA29858B1 (fr) | Derives de carbamoylbenzotriazole en tant qu'inhibiteurs de lipases et phospholipases | |
| MA29856B1 (fr) | Derives de diacylindazole en tant qu'inhibiteurs de lipases et de phospholipases | |
| MA30291B1 (fr) | Derives de l'azolopyridin-3-one en tant qu'inhibiteurs de la lipase endotheliale | |
| MA29909B1 (fr) | Derives de pyridazine | |
| MA29393B1 (fr) | Derives d'azole sous forme d'inhibiteurs de lipase et de phospholipase | |
| MA31433B1 (fr) | Inhibiteurs de la p70 s6 kinase | |
| MA31574B1 (fr) | Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf | |
| MA34819B1 (fr) | Dérivés bicyclo[3.2.1]octylamide et leurs utilisations | |
| MA27559A1 (fr) | Nouveaux derives de fluorglycoside aromatiques, produits pharmaceutiques contenant ces composes et leur utilisation | |
| MXPA05008172A (es) | Derivados de malonamida como inhibidores gamma-secretasa. | |
| MA32929B1 (fr) | Lactames en tant qu'inhibiteurs de bêta-sécrétase | |
| MA33384B1 (fr) | Sulfonamides hétérocycliques, leurs utilisations et compositions pharmaceutiques les contenant | |
| CY1111170T1 (el) | Ενωσεις διαρυλ αιθερα ουριας | |
| MA34169B1 (fr) | Dérivés d'acide 1-amino-2-cyclopropyléthylboronique | |
| MA35749B1 (fr) | Dérivés nucléosidiques 4'-azido, 3'-fluoro substitués en tant qu'inhibiteurs de la réplication de l'arn du vhc | |
| MA31903B1 (fr) | Derives de thiazole utilises comme inhibiteur de la pi 3 kinase | |
| MA31295B1 (fr) | 5-oxo-isoxazoles en tant qu'inhibiteurs de lipases et de phospholipases | |
| MA30609B1 (fr) | Imidazolidine-2,4-diones arylaminoaryl-alkyl-substituees, leur procede de synthese, les medicaments comprenant ces composes, et leurs applications. | |
| MA47301B1 (fr) | Inhibiteurs sélectifs de jak1 | |
| MA30821B1 (fr) | Derives de pyrazoline utiles comme antagonistes des recepteurs de mineralocorticoïdes | |
| MA31873B1 (fr) | Inhibiteurs de la peptide déformylase | |
| TN2013000393A1 (fr) | Derives de la pyrazolospirocetone pour une utilisation comme inhibiteurs de l'acetyl-coa carboxylase | |
| EP2058317A4 (fr) | Dérivé d'ester de l'acide aminophosphorique et modulateur de récepteur s1p contenant le dit dérivé en tant que principe actif |